Canonical Allele Identifier: PA286509
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102850
ClinVar RCV Id: RCV000089109 RCV000758132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.His271Arg
CA286508
NM_000277.3:c.812A>G